Kawamura Rie 河村理恵

… Alternative Names

河村理恵カワムラリエ

KAWAMURA Rie 河村理恵

Less

Researcher Number	20735534
Other IDs
Affiliation (Current)	2025: 藤田医科大学, 医科学研究センター, 助教
Affiliation (based on the past Project Information) *help	2023: 藤田医科大学, 医科学研究センター, 助教 2018 – 2021: 藤田医科大学, 総合医科学研究所, 助教 2015 – 2017: 信州大学, 医学部, 助教(特定雇用)
Review Section/Research Field	Principal Investigator Basic Section 50010:Tumor biology-related / Learning support system Except Principal Investigator Basic Section 56040:Obstetrics and gynecology-related / Human genetics
Keywords	Principal Investigator 核内トポロジー / 染色体再構成 / 核内配置編集 / 染色体配置編集 / ゲノム編集 / 染色体配置 / マイクロアレイ染色体検査 / 教材開発 / 染色体検査 / 遺伝医学 / cytogenetics / 細胞遺伝 / 遺伝学的検査 … More Except Principal Investigator … More 着床前遺伝学的検査 / 初期胚 / モザイク / 着床前染色体検査 / 染色体異常 / エピジェネティック / 1細胞解析 / X染色体不活化 / エピジェネティクス / RNA-FISH / 相同染色体 / １細胞解析 Less

染色体の核内配置編集による染色体転座の発生機序の解明Principal Investigator
- Principal Investigator
  
  河村理恵
- Project Period (FY)
  2023 – 2025
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 50010:Tumor biology-related
- Research Institution
  Fujita Health University
Risk factors related to chromosomal aneuploidy in human blastocysts
- Principal Investigator
  
  Miyai Shunsuke
- Project Period (FY)
  2019 – 2021
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 56040:Obstetrics and gynecology-related
- Research Institution
  Fujita Health University
Development of a hands-on cytogenetics training program for genomic medical workersPrincipal Investigator
- Principal Investigator
  
  KAWAMURA Rie
- Project Period (FY)
  2017 – 2019
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Learning support system
- Research Institution
  Fujita Health University
  Shinshu University
Research for single cell expression analysis and epigenetic mechanism using RNA-FISH analyses
- Principal Investigator
  
  Wakui Keiko
- Project Period (FY)
  2015 – 2017
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Human genetics
- Research Institution
  Shinshu University

All 2023 2020 2019 2018 2017 2016 2015

All Journal Article Presentation

[Journal Article] A case of a parthenogenetic 46,XX/46,XY chimera presenting ambiguous genitalia.2020
- Author(s)
  Kawamura R, Kato T, Miyai S, Suzuki F, Naru Y, Kato M, Tanaka K, Nagasaka M, Tsutsumi M, Inagaki H, Ioroi T, Yoshida M, Nao T, Conlin LK, Iijima K, Kurahashi H, Taniguchi-Ikeda M.
- Journal Title
  
  J Hum Genet.
  
  Volume: - Issue: 8 Pages: 705-709
- DOI
  10.1038/s10038-020-0748-4
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K09790, KAKENHI-PROJECT-17K00481, KAKENHI-PROJECT-17K11259
[Journal Article] Exome-First Approach in Fetal Akinesia Reveals Chromosome 1p36 Deletion Syndrome.2019
- Author(s)
  Toshimitsu M, Nagaoka S, Kobori S, Ogawa M, Suzuki F, Kato T, Miyai S, Kawamura R, Inagaki H, Kurahashi H, Murotsuki J.
- Journal Title
  
  Case Rep Obstet Gynecol.
  
  Volume: - Pages: 1-5
- DOI
  10.1155/2019/6753184
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K09790, KAKENHI-PROJECT-17K11259
[Journal Article] CTCF deletion syndrome: Clinical features and epigenetic delineation2017
- Author(s)
  Hori I, Kawamura R, Nakabayashi K, Watanabe H, Higashimoto K, Tomikawa J, Ieda D, Ohashi K, Negishi Y, Hattori A, Sugio Y, Wakui K, Hata K, Soejima H, Kurosawa K, Saitoh S
- Journal Title
  
  Journal of Medical Genetics
  
  Volume: 54 Issue: 12 Pages: 836-842
- DOI
  10.1136/jmedgenet-2017-104854
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K07248, KAKENHI-PROJECT-17K08687, KAKENHI-PROJECT-26293365, KAKENHI-PROJECT-15K08330
[Presentation] Presence of small 21p-21p chromosome in mosaic rob(21;21) carrier2023
- Author(s)
  Rie Kawamura, Ikumi Moriyama, Shunsaku Fujii, Takeshi Iwasa, Akira Kuwahara, Minoru Irahara, Ei Yuzawa, Hiroki Kurahashi
- Organizer
  日本人類遺伝学会　第68回大会
- Data Source
  KAKENHI-PROJECT-23K06619
[Presentation] 全ゲノムシークエンスで同定されたエンハンサー領域欠失によるOTC欠損症の１例2023
- Author(s)
  河村理恵,中島葉子,稲垣秀人,七里由衣,村瀬悠理,倉橋浩樹
- Organizer
  第46回日本小児遺伝学会　学術集会
- Data Source
  KAKENHI-PROJECT-23K06619
[Presentation] Genetic counseling for preimplantation genetic diagnosis2019
- Author(s)
  河村理恵，森山育実，加藤麻希，河合美紀，宮井俊輔，倉橋浩樹
- Organizer
  第43回日本遺伝カウンセリング学会学術集会
- Data Source
  KAKENHI-PROJECT-19K09790
[Presentation] dic(Y;22)と45,Xの核型をもつターナー症候群の一例2019
- Author(s)
  河村理恵，稲垣秀人，山田緑，鈴木史彦，成悠希，倉橋浩樹
- Organizer
  日本人類遺伝学会第64回大会
- Data Source
  KAKENHI-PROJECT-17K00481
[Presentation] Parthenogenetic maternalとdouble paternal alleleを有するキメラ症例の解析2019
- Author(s)
  河村理恵，加藤武馬，宮井俊輔，鈴木史彦，成悠希，田中敬子，長坂美和子，池田真理子，倉橋浩樹
- Organizer
  第41回日本小児遺伝学会学術集会
- Data Source
  KAKENHI-PROJECT-17K00481
[Presentation] 着床前診断を希望して来談されたクライエントの想いと遺伝カウンセリング2019
- Author(s)
  河村理恵，森山育実，加藤麻希，河合美紀，宮井俊輔，倉橋浩樹
- Organizer
  第43回日本遺伝カウンセリング学会学術集会
- Data Source
  KAKENHI-PROJECT-17K00481
[Presentation] Report of a 46,XX/46,XY with parthenogenetic chimera2018
- Author(s)
  河村理恵，加藤武馬，宮井俊輔，鈴木史彦，成悠希，田中敬子，長坂美和子，池田真理子，倉橋浩樹
- Organizer
  日本人類遺伝学会第63回大会
- Data Source
  KAKENHI-PROJECT-17K00481
[Presentation] マイクロアレイ染色体検査にて派生染色体に端部欠失が検出されなかった不均衡型転座症例2017
- Author(s)
  河村理恵
- Organizer
  日本人類遺伝学会第62回大会
- Data Source
  KAKENHI-PROJECT-17K00481
[Presentation] CTCF遺伝子欠失を認めた2女児の臨床的および遺伝学的検討2016
- Author(s)
  堀いくみ, 河村理恵, 中林一彦, 家田大輔, 大橋圭, 根岸豊, 服部文子, 杉尾嘉嗣, 涌井敬子, 黒澤健司, 秦健一郎, 副島英伸, 齋藤伸治
- Organizer
  第39回日本小児遺伝学会学術集会
- Place of Presentation
  慶應義塾大学三田北館ホール
- Year and Date
  2016-12-09
- Data Source
  KAKENHI-PROJECT-15K08330
[Presentation] Xp21欠失女性症例における不活化X染色体解析　 ―構造異常X染色体を識別するRNA/DNA-FISH解析―2015
- Author(s)
  河村理恵，伊波若葉，福嶋義光，涌井敬子
- Organizer
  日本人類遺伝学会第60回大会
- Place of Presentation
  京王プラザホテル（新宿・東京）
- Year and Date
  2015-10-14
- Data Source
  KAKENHI-PROJECT-15K08330
[Presentation] Establishment of a single-cell RNA/DNA-FISH method for detecting inactivation patterns of structural X chromosome abnormalities2015
- Author(s)
  Rie KAWAMURA, Wakaba IHA, Yoshimitsu FUKUSHIMA, Keiko WAKUI
- Organizer
  第10回European Cytogenetics Conference
- Place of Presentation
  ストラスブール（フランス）
- Year and Date
  2015-07-04
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K08330

1. Wakui Keiko (50324249)

# of Collaborated Projects: 2 results

# of Collaborated Products: 3 results
2. 福嶋義光 (70273084)

# of Collaborated Projects: 2 results

# of Collaborated Products: 2 results
3. KOSHO Tomoki (90276311)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
4. SAITOH Shinji (00281824)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
5. Miyai Shunsuke (50563350)

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
6. 高野亨子 (70392420)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
7. 加藤武馬 (20387690)

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
8. 稲垣秀人 (70308849)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
9. 倉橋浩樹 (30243215)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
10. 斉藤伸治

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
11. 冨川順子

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

Kawamura Rie 河村 理恵

河村 理恵 カワムラ リエ

KAWAMURA Rie 河村 理恵

Research Projects

Research Products

Co-Researchers

染色体の核内配置編集による染色体転座の発生機序の解明Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Risk factors related to chromosomal aneuploidy in human blastocysts

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Development of a hands-on cytogenetics training program for genomic medical workersPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Research for single cell expression analysis and epigenetic mechanism using RNA-FISH analyses

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] A case of a parthenogenetic 46,XX/46,XY chimera presenting ambiguous genitalia.2020

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Exome-First Approach in Fetal Akinesia Reveals Chromosome 1p36 Deletion Syndrome.2019

Author(s)

Journal Title

DOI

Data Source

[Journal Article] CTCF deletion syndrome: Clinical features and epigenetic delineation2017

Author(s)

Journal Title

DOI

Data Source

[Presentation] Presence of small 21p-21p chromosome in mosaic rob(21;21) carrier2023

Author(s)

Organizer

Data Source

[Presentation] 全ゲノムシークエンスで同定されたエンハンサー領域欠失によるOTC欠損症の１例2023

Author(s)

Organizer

Data Source

[Presentation] Genetic counseling for preimplantation genetic diagnosis2019

Author(s)

Organizer

Data Source

[Presentation] dic(Y;22)と45,Xの核型をもつターナー症候群の一例2019

Author(s)

Organizer

Data Source

[Presentation] Parthenogenetic maternalとdouble paternal alleleを有するキメラ症例の解析2019

Author(s)

Organizer

Data Source

[Presentation] 着床前診断を希望して来談されたクライエントの想いと遺伝カウンセリング2019

Author(s)

Organizer

Data Source

[Presentation] Report of a 46,XX/46,XY with parthenogenetic chimera2018

Author(s)

Organizer

Data Source

[Presentation] マイクロアレイ染色体検査にて派生染色体に端部欠失が検出されなかった不均衡型転座症例2017

Author(s)

Organizer

Data Source

[Presentation] CTCF遺伝子欠失を認めた2女児の臨床的および遺伝学的検討2016

Author(s)

Organizer

Kawamura Rie 河村理恵

河村理恵カワムラリエ

KAWAMURA Rie 河村理恵

[Presentation] Xp21欠失女性症例における不活化X染色体解析　 ―構造異常X染色体を識別するRNA/DNA-FISH解析―2015